Canonical Allele Identifier: PA916034570
Gene: ATM HGNC NCBI
ClinVar RCV:
RCV000003167
ClinVar Variation:
3028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2656Pro
CA115935
NM_001351834.2:c.7967T>C